Aqueous Pigment Preparations Having Nonionic Additives on the Basis of Alyl and Vinyl Ether

ABSTRACT

The invention relates to an aqueous pigment preparation, containing (A) at least one organic and/or inorganic pigment, (B) a dispersing agent of the formulas (I), (II), (III), or (IV), or mixtures of the dispersing agent of the formulas (I), (II), (III), or (IV), (C) optionally a wetting agent, (D) optionally further surfactants and/or dispersing agents, (E) optionally one or multiple organic solvents, or one or multiple hydrotropic substances, (F) optionally further additives common for the production of aqueous pigment dispersions, and (G) water.

The present invention provides aqueous pigment preparations comprising novel nonionic polymers as dispersants and also their use for coloration of natural and synthetic materials.

Dispersing pigments in liquid media typically requires dispersants. Examples of where dispersants are of particular commercial importance are the dispersing of pigments in the manufacture of pigment concentrates (used for coloration of emulsion and varnish colors, paints, coatings and printing inks) and also the coloration of paper, cardboard and textiles.

Pigment preparations comprising ordered polymeric structures are also described in the prior art. Examples thereof are EP 1 293 523, DE 10 2005 012 315 and EP 1 721 941.

The formerly customary novolak dispersants contain as a consequence of their process of production residues of alkylphenols, frequently nonylphenol, and ethoxylates thereof. Since alkylphenol ethoxylates, or their degradation products, scarcely undergo any degradation in the environment, they build up. This is problematic in that they have a hormonal effect on aquatic organisms. Therefore, many countries have adopted legislation (2003/53/EC for example) which limits or bans the use of materials containing alkylphenols or their ethoxylates in open-loop systems.

Studies to date have shown that it is still extremely difficult to synthesize dispersants that are equivalent in performance to nonionic novolak systems. There is accordingly a need for novel dispersants that are capable of dispersing organic pigments in high concentration above 40% to low-viscosity dispersions. These dispersions shall be straightforward to produce; i.e., the pigments shall be readily wetted and be readily incorporated into the aqueous medium. The dispersion shall have a high and reproducible color strength and this shall remain stable for a period of several years. Similarly, all further coloristic parameters such as, for example, hue angle and chroma shall be reproducible and stable. Furthermore, the dispersion shall have a low viscosity; the pigments must neither agglomerate nor flocculate, nor cream up or form a sediment. The dispersion should not foam or cause or speed foaming in the application medium. Furthermore, the dispersants should contribute to broad compatibility of the dispersions in various application media. Moreover, the dispersion shall be shear stable; i.e., its color strength or coloristics must not change under shearing, and the dispersion shall remain resistant to flocculation under these conditions.

It has now been found that, surprisingly, specific nonionic comb copolymers, prepared by means of macromonomers composed of polyethylene/polypropylene glycol monovinyl ethers or monoallyl ethers, achieve this object.

The present invention provides aqueous pigment preparations comprising

-   (A) at least one organic and/or inorganic pigment, -   (B) a dispersant of formula (I), (II), (III) or (IV) or mixtures of     dispersants of formulae (I), (II), (III) or (IV)

where the indices a, b and c indicate the molar fraction of the respective monomers

-   a=0.01 to 0.8, preferably 0.1 to 0.7; -   b=0.001 to 0.8, preferably 0.1 to 0.6; -   c=0.001 to 0.8, preferably 0.1 to 0.6;     provided the sum total of a+b+c is 1, -   A represents C₂- to C₄-alkylene and -   B represents a C₂- to C₄-alkylene other than A, -   k equals 0 or 1, -   m is from 0 to 500, preferably from 0 to 50; -   n is from 0 to 500, preferably from 0 to 50,     provided the sum total of m+n is from 1 to 1000; -   X_(a) represents an aromatic or araliphatic radical having 3 to 30     carbon atoms which optionally contains one or more of the hetero     atoms N, O and S, -   Z_(a) represents H or (C₁-C₄)-alkyl, -   Z_(b) represents H or (C₁-C₄)-alkyl, -   Z_(c) represents H or (C₁-C₄)-alkyl; -   R¹ represents hydrogen or methyl, -   X_(b) represents an aromatic or araliphatic radical having 3 to 30     carbon atoms which optionally contains one or more of the hetero     atoms N, O and S, -   W_(a) represents oxygen or an NH group, -   R² represents hydrogen or methyl, -   Y represents an aliphatic hydrocarbyl radical having 1 to 30 carbon     atoms, preferably 6 to 30, particularly 9 to 20 carbon atoms, which     may be linear or branched or else cyclic, and which may contain     hetero atoms O, N and/or S and may also be unsaturated, -   W_(b) represents oxygen or an NH group; -   (C) optionally wetters, -   (D) optionally further surfactants and/or dispersants, -   (E) optionally one or more organic solvents and/or one or more     hydrotropic substances, -   (F) optionally further additive materials customary for preparing     aqueous pigment dispersions, and -   (G) water.

Preferred pigment preparations comprise 5% to 80% by weight, for example 10% to 70% by weight, of component (A).

-   Preferred pigments preparations comprise 0.1% to 30% by weight, for     example 2% to 15% by weight of component (B).

Particularly preferred pigment preparations comprise in terms of component

-   (A) 5% to 80% by weight, for example 10% to 70% by weight, -   (B) 0.1% to 30% by weight, for example 2% to 15% by weight, -   (C) 0% to 10% by weight, for example 0.1% to 5% by weight, -   (D) 0% to 20% by weight, for example 1% to 10% by weight, -   (E) 0% to 30% by weight, for example 5% to 20% by weight, -   (F) 0% to 20% by weight, for example 0.1% to 5% by weight, -   (G) 1% to 90% by weight of water, for example 10% to 70% by weight,     all based on the total weight (100% by weight) of the pigment     preparation.

When one or more of components (C), (D), (E) and (F) are present, their minimum concentrations independently of each other are preferably at least 0.01% by weight and more preferably at least 0.1% by weight, based on the total weight of the pigment preparation.

Component (A) in the pigment preparation of the present invention is a finely divided organic or inorganic pigment or a mixture of various organic and/or inorganic pigments. Component (A) can also be a dye that is soluble in certain solvents and has pigment character in other solvents. The pigments can be used not only in the form of dry powder but also as water-moist presscake.

Useful organic pigments include monoazo, disazo, laked azo, β-naphthol, Naphthol AS, benzimidazolone, disazo condensation, azo metal complex pigments or polycyclic pigments such as, for example, the phthalocyanine, quinacridone, perylene, perinone, thioindigo, anthanthrone, anthraquinone, flavanthrone, indanthrone, isoviolanthrone, pyranthrone, dioxazine, quinophthalone, isoindolinone, isoindoline and diketopyrrolopyrrole pigments or carbon blacks.

Of the organic pigments mentioned, those which are in a very fine state of subdivision for producing the preparations are particularly suitable, and preferably 95% and more preferably 99% of the pigment particles have a particle size≦500 nm.

An exemplary selection of particularly preferred organic pigments includes carbon black pigments, for example lamp or furnace blacks; monoazo and disazo pigments, in particular the Colour Index pigments Pigment Yellow 1, Pigment Yellow 3, Pigment Yellow 12, Pigment Yellow 13, Pigment Yellow 14, Pigment Yellow 16, Pigment Yellow 17, Pigment Yellow 73, Pigment Yellow 74, Pigment Yellow 81, Pigment Yellow 83, Pigment Yellow 87, Pigment Yellow 97, Pigment Yellow 111, Pigment Yellow 126, Pigment Yellow 127, Pigment Yellow 128, Pigment Yellow 155, Pigment Yellow 174, Pigment Yellow 176, Pigment Yellow 191, Pigment Yellow 213, Pigment Yellow 214, Pigment Yellow 219, Pigment Red 38, Pigment Red 144, Pigment Red 214, Pigment Red 242, Pigment Red 262, Pigment Red 266, Pigment Red 269, Pigment Red 274, Pigment Orange 13, Pigment Orange 34 or Pigment Brown 41; 3-naphthol and Naphthol AS pigments, in particular the Colour Index pigments Pigment Red 2, Pigment Red 3, Pigment Red 4, Pigment Red 5, Pigment Red 9, Pigment Red 12, Pigment Red 14, Pigment Red 53:1, Pigment Red 112, Pigment Red 146, Pigment Red 147, Pigment Red 170, Pigment Red 184, Pigment Red 187, Pigment Red 188, Pigment Red 210, Pigment Red 247, Pigment Red 253, Pigment Red 256, Pigment Orange 5, Pigment Orange 38 or Pigment Brown 1; laked azo and metal complex pigments, in particular the Colour Index pigments Pigment Red 48:2, Pigment Red 48:3, Pigment Red 48:4, Pigment Red 57:1, Pigment Red 257, Pigment Orange 68 or Pigment Orange 70; benzimidazoline pigments, in particular the Colour Index pigments Pigment Yellow 120, Pigment Yellow 151, Pigment Yellow 154, Pigment Yellow 175, Pigment Yellow 180, Pigment Yellow 181, Pigment Yellow 194, Pigment Red 175, Pigment Red 176, Pigment Red 185, Pigment Red 208, Pigment Violet 32, Pigment Orange 36, Pigment Orange 62, Pigment Orange 72 or Pigment Brown 25; isoindolinone and isoindoline pigments, in particular the Colour Index pigments Pigment Yellow 139 or Pigment Yellow 173; phthalocyanine pigments, in particular the Colour Index pigments Pigment Blue 15, Pigment Blue 15:1, Pigment Blue 15:2, Pigment Blue 15:3, Pigment Blue 15:4, Pigment Blue 15:6, Pigment Blue 16, Pigment Green 7 or Pigment Green 36; anthanthrone, anthraquinone, quinacridone, dioxazine, indanthrone, perylene, perinone and thioindigo pigments, in particular the Colour Index pigments Pigment Yellow 196, Pigment Red 122, Pigment Red 149, Pigment Red 168, Pigment Red 177, Pigment Red 179, Pigment Red 181, Pigment Red 207, Pigment Red 209, Pigment Red 263, Pigment Blue 60, Pigment Violet 19, Pigment Violet 23 or Pigment Orange 43; triarylcarbonium pigments, in particular the Colour Index pigments Pigment Red 169, Pigment Blue 56 or Pigment Blue 61; diketopyrrolopyrrole pigments, in particular the Colour Index pigments Pigment Red 254, Pigment Red 255, Pigment Red 264, Pigment Red 270, Pigment Red 272, Pigment Orange 71, Pigment Orange 73, Pigment Orange 81.

Laked dyes such as calcium, magnesium and aluminum lakes of sulfonated and/or carboxylated dyes are also suitable.

Suitable inorganic pigments include for example titanium dioxides, zinc sulfides, zinc oxides, iron oxides, magnetites, manganese iron oxides, chromium oxides, ultramarine, nickel or chromium antimony titanium oxides, manganese titanium rutiles, cobalt oxides, mixed oxides of cobalt and of aluminum, rutile mixed phase pigments, sulfides of the rare earths, spinets of cobalt with nickel and zinc, spinets based on iron and chromium with copper zinc and also manganese, bismuth vanadates and also blend pigments. The Colour Index pigments Pigment Yellow 184, Pigment Yellow 53, Pigment Yellow 42, Pigment Yellow Brown 24, Pigment Red 101, Pigment Blue 28, Pigment Blue 36, Pigment Green 50, Pigment Green 17, Pigment Black 11, Pigment Black 33 and also Pigment White 6 are used in particular. Preference is frequently also given to using mixtures of inorganic pigments. Mixtures of organic with inorganic pigments are likewise often used.

Instead of pigment dispersions it is also possible to prepare dispersions of solids including for example natural finely divided ores, minerals, sparingly soluble or insoluble salts, particles of wax or plastic, dyes, crop protection and pest control agents, UV absorbers, optical brighteners and polymerization stabilizers.

The copolymers (component B) have a molecular weight of 10³ g/mol to 10⁹ g/mol, more preferably of 10³ to 10⁷ g/mol and even more preferably 10³ to 10⁵ g/mol. These polymers may be prepared by free-radical polymerization of monomers corresponding to the radicals in formula (I), (II), (III) or (IV) which are described in the parentheses [ ]_(c), [ ]_(b) and [ ]_(a). The conditions for performing the free-radical polymerization are known to those skilled in the art.

Preferred monomers of group [ ]_(a) are those in which A is ethylene and B is propylene, or A is propylene and B is ethylene.

The alkylene oxide units (A-O)_(m) and (B—O)_(n) can be present either in a random arrangement or, as in the case of a preferred embodiment, in a blocklike arrangement.

The sum total of the alkylene oxide units can in principle be n+m=1 to 1000, although 1 to 500 is preferred, 2 to 100 is particularly preferred and 5 to 100 is even more particularly preferred.

The monomers of group [ ]_(b) include for example the following esters and amides of acrylic acid and methacrylic acid: phenyl, benzyl, tolyl, 2-phenoxyethyl, phenethyl.

Monomers of group [ ]_(b) further include vinylaromatic monomers such as styrene and its derivatives, such as vinyltoluene and α-methylstyrene for example. The aromatic unit may also comprise heteroaromatics, as in 1-vinylimidazole for example.

Particularly preferred monomers of group [ ]_(b) can be: styrene, 1-vinylimidazole, benzyl methacrylate, 2-phenoxyethyl methacrylate and phenethyl methacrylate.

The monomers of group [ ]_(c) include for example the following esters and amides of acrylic acid and methacrylic acid: methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, t-butyl, pentyl, hexyl, 2-ethylhexyl, 3,3-dimethylbutyl, heptyl, octyl, isooctyl, nonyl, lauryl, cetyl, stearyl, behenyl, cyclohexyl, trimethylcyclohexyl, t-butylcyclohexyl, bornyl, isobornyl, adamantyl, (2,2-dimethyl-1-methyl)propyl, cyclopentyl, 4-ethyl-cyclohexyl, 2-ethoxyethyl, tetrahydrofurfuryl and tetrahydropyranyl.

The monomers of group [ ]_(c) further include the vinyl esters of carboxylic acids, such as for example vinyl laurate, vinyl myristate, vinyl stearate, vinyl behenate, vinyl pivalate, vinyl neohexanoate, vinyl neoheptanoate, vinyl neooctanoate, vinyl neononanoate and vinyl neodecanoate. The vinyl esters of mixtures of such carboxylic acids can likewise be used here.

Preferred monomers of group [ ]_(c) are the following alkyl esters and alkylamides of acrylic acid and methacrylic acid: methyl, ethyl, propyl, butyl, isobutyl, 2-ethoxyethyl, myristyl, octadecyl, more preferably 2-ethylhexyl and lauryl.

Component (C) generally comprises cationic, anionic, amphoteric or nonionic compounds which enhance pigment wetting (wetting agents, wetters), for example, alkyl sulfates such as, for example, lauryl sulfate, alkylbenzene sulfonic acid, short-chain alkoxylation products such as, for example, lauryl alcohol reacted with approximately 5 mol of ethylene oxide or alkynediols.

Component (D) in the pigment preparations of the present invention comprises customary dispersants and surfactants useful for preparing aqueous pigment dispersions, or mixtures thereof. Anionic, cationic, amphoteric or nonionic surface-active compounds are typically used, as described in DE-A-10 2007 021 870.

Component (E) comprises organic solvents or water-soluble hydrotropic substances. Hydrotropic compounds, which also serve as a solvent, if appropriate, or are oligomeric or polymeric in nature are for example formamide, urea, tetra-methylurea, ε-caprolactam, ethylene glycol, propylene glycol, diethylene glycol, triethylene glycol, polyethylene glycol, α-methyl ω-hydroxy polyethylene glycol ether, dimethyl polyethylene glycol ether, dipropylene glycol, polypropylene glycol, dimethyl polypropylene glycol ether, copolymers of ethylene glycol and propylene glycol, butyl glycol, methylcellulose, glycerol, diglycerol, polyglycerol, N-methyl-pyrrolidone, 1,3-diethyl-2-imidazolidinone, thiodiglycol, sodium benzenesulfonate, sodium xylenesulfonate, sodium toluenesulfonate, sodium cumenesulfonate, sodium dodecylsulfonate, sodium benzoate, sodium salicylate, sodium butyl monoglycol sulfate, cellulose derivatives, gelatin derivatives, polyvinylpyrrolidone, polyvinyl alcohol, polyvinylimidazole and co- and terpolymers of vinylpyrrolidone, vinyl acetate and vinylimidazole. Polymers comprising vinyl acetate building blocks may subsequently be saponified to the vinyl alcohol.

Component (F) comprises for example thickeners, preservatives, viscosity stabilizers, grinding assistants and fillers. Further customary additives are antisettling agents, photoprotectants, antioxidants, degassers/defilmers, foam-reducing agents, anticaking agents and also viscosity and rheology improvers. Useful viscosity regulators include for example polyvinyl alcohol and cellulose derivatives. Water-soluble natural or manufactured resins and also polymers may similarly be included as filming or binding agents to enhance bonding strength and abrasion resistance. Useful pH regulators include organic or inorganic bases and acids. Preferred organic bases are amines, for example ethanolamine, diethanolamine, triethanolamine, N,N-dimethylethanolamine, diisopropylamine, aminomethylpropanol or dimethylaminomethylpropanol. Preferred inorganic bases are sodium hydroxide, potassium hydroxide, lithium hydroxide or ammonia. Component (F) further comprises fats and oils of vegetable and animal origin, for example beef tallow, palm kernel fat, coconut fat, rapeseed oil, sunflower oil, linseed oil, palm oil, soy oil, groundnut oil and whale oil, cotton seed oil, maize oil, poppy seed oil, olive oil, castor oil, colza oil, safflower oil, soybean oil, thistle oil, sunflower oil, herring oil, sardine oil. Common additives also include saturated and unsaturated higher fatty acids, for example palmitic acid, cyprylic acid, capric acid, myristic acid, lauric acid, stearic acid, oleic acid, linoleic acid, linolenic acid, caproic acid, caprylic acid, arachidic acid, behenic acid, palmitoleic acid, gadoleic acid, erucic acid and ricinoleic acid, and also salts thereof.

Water used as component (G) to produce the pigment preparations is preferably used in the form of demineralized or distilled water. It is similarly possible to use drinking water (tap water) and/or water of natural origin.

The present invention also provides a process for producing the pigment preparations of the present invention, which process comprises dispersing said component (A) in the form of powder, granulate or aqueous presscake in the presence of water (G) and also said components (B) and optionally (C) and (D), then optionally admixing water (G) and also optionally one or more of said components (E) and (F) and optionally diluting the resulting aqueous pigment dispersion with water (G). Said components (B) and optionally one or more of said components (C), (D), (E) and (F) are preferably initially mixed and homogenized, then said component (A) is stirred into the initially charged mixture, said component (A) being incipiently pasted and predispersed. The predispersion is subsequently, depending on the texture of component (A), finely dispersed or finely dissipated, with or without cooling, using a grinding or dispersing assembly. Such may include stirrers, dissolvers (sawtooth stirrers), rotor-stator mills, ball mills, stirred media mills such as sand and bead mills, high speed mixers, kneaders, roll stands or high performance bead mills. The fine dispersing or grinding of component (A) is carried on to the desired particle size distribution and can take place at temperatures in the range from 0 to 100° C., advantageously at a temperature between 10 and 70° C., preferably at 20 to 60° C. Following the fine-dispersing operation, the pigment preparation may be further diluted with water (G), preferably deionized or distilled water.

The pigment preparations of the present invention are useful for pigmentation and coloration of natural and synthetic materials of any kind, particularly of aqueous paints, emulsion and varnish colors (emulsion varnishes).

The pigment preparations of the present invention are further useful for coloration of macromolecular materials of any kind, for example of natural and synthetic fiber materials, preferably cellulose fibers, and also for paper pulp coloration and for laminate coloration. Further uses are the production of printing colors, for example textile printing colors, flexographic printing inks, decorative printing inks or intaglio printing inks, wallpaper colors, water-thinnable coatings, wood preservation systems, viscose dope dyeing systems, varnishes, including powder coatings, sausage casings, seed, fertilizers, glass, particularly glass bottles, and also of mass coloration of roof shingles, for coloration of renders, concrete, wood stains, colored pencil leads, felt tip pens, waxes, paraffins, graphics inks, ball point pen pastes, chalks, washing and cleaning compositions, shoe care agents, latex products, abrasives, and also for coloration of plastics or high molecular weight materials of any kind. Examples of high molecular weight organic materials are cellulose ethers and esters, such as ethylcellulose, nitrocellulose, cellulose acetate or cellulose butyrate, natural resins or synthetic resins, such as addition polymerization resins or condensation resins, for example amino resins, particularly urea- and melamine-formaldehyde resins, alkyd resins, acrylic resins, phenolic resins, polycarbonates, polyolefins, such as polystyrene, polyvinyl chloride, polyethylene, polypropylene, polyacrylonitrile, polyacrylic esters, polyamides, polyurethanes or polyesters, rubber, casein, lattices, silicone, silicone resins, individually or in admixture.

The pigment preparations of the present invention are further useful for producing liquid printing inks for use in all conventional ink-jet printers, particularly for those based on the bubble jet or piezo process. These liquid printing inks can be used to print paper and also natural or synthetic fiber materials, foils and plastics.

Additionally, the pigment preparations of the present invention can be used for printing various kinds of coated or uncoated substrate materials, for example for printing paper board, cardboard, wood and woodbase materials, metallic materials, semiconductor materials, ceramic materials, glasses, glass and ceramic fibers, inorganic materials of construction, concrete, leather, comestibles, cosmetics, skin and hair. The substrate material may be two-dimensionally planar or spatially extended, i.e., three-dimensionally configured, and may be printed or coated completely or only in parts.

The pigment preparations of the present invention are also useful as a colorant in electrophotographic toners and developers, for example in one- or two-component powder toners (also called one- or two-component developers), magnet toners, liquid toners, latex toners, polymerization toners and also specialty toners.

The pigment preparations of the present invention are also useful as a colorant in liquid inks, preferably ink-jet inks, for example aqueous or nonaqueous (solvent based), microemulsion inks, UV-curable inks, and also in such inks that operate according to the hot melt process.

The pigment preparations of the present invention can also be used as colorants for color filters for flat panels displays, not only for additive but also for subtractive color production, also for photoresists and also as colorants for “electronic inks” or “e-inks” or “electronic paper” or “e-paper”.

EXAMPLES Preparation of Dispersants (B) Synthesis Prescription 1

A flask equipped with stirrer, reflux condenser, internal thermometer and nitrogen inlet was initially charged with monomer A, monomer C and, where appropriate, the molecular weight regulator in solvent under nitrogen.

Then, the temperature was raised to 80° C. with stirring and a solution of the initiator was added during one hour by metering. At the same time, the metered addition was commenced of monomer B, and it was concluded after 3 hours. The batch was subsequently further stirred at this temperature for 2 hours, and then the solvent was removed under reduced pressure.

Synthesis Prescription 2

A flask equipped with stirrer, reflux condenser, internal thermometer and nitrogen inlet was initially charged with monomer A, monomer C and, where appropriate, the molecular weight regulator and component 1 (ascorbic acid) of the redox initiator system in solvent under nitrogen. Then, the temperature was raised to 80° C. with stirring and a solution of component 2 (t-BuOOH) of the redox initiator system was added during three hours with stirring. At the same time the metered addition was commenced of monomer B, and it was concluded after 3 hours. The batch was subsequently further stirred at this temperature for 2 hours, and then the solvent was removed under reduced pressure.

The following three tables contain synthesis examples carried out similarly to the above two general synthesis prescriptions.

AMBN=2,2′-azobis(2-methylbutyronitrile)

TABLE 1 1 2 3 4 5 6 7 8 9 10 Monomer C 2-ethylhexyl methacrylate 136.4 g  lauryl methacrylate 175.0 g  stearyl methacrylate 232.8 g  isobornyl methacrylate 152.9 g  tetrahydrofurfuryl 117.1 g  methacrylate vinyl neononanoate 78.3 g 78.3 g vinyl neodecanoate 84.3 g 84.3 g vinyl neoundecanoate 90.3 g Monomer B 1-vinylimidazole 64.7 g 64.7 g styrene 71.6 g 41.6 g 41.6 g 41.6 g benzyl methacrylate 70.4 g 70.4 g phenethyl methacrylate 130.8 g  2-phenoxyethyl 141.8 g  methacrylate Monomer A polyglcyol 1  300 g  300 g  300 g  300 g polyglycol 2 378.4 g  378.4 g  378.4 g  378.4 g  polyglycol 3  688 g polyglycol 4 3000 g  Initiator AMBN 16.5 g 13.4 g 13.4 g 16.5 g 13.4 g 16.5 g 13.4 g dibenzoyl peroxide 20.8 g ascorbic acid/t-BuOOH 17.51 g/ 17.51 g/ 7.73 g 7.73 g Regulator dodecanethiol 16.5 g 16.5 g 16.5 g 16.5 g 16.5 g 13.4 g ethyl mercaptan  4.2 g Solvent methyl ethyl ketone  660 g  660 g  660 g  660 g  660 g  660 g methyl isobutyl ketone  660 g  660 g isopropanol  660 g  660 g to synthesis 1 1 1 1 1 1 1 1 2 2 prescription . . . M_(w) of polymer obtained 14000 18500 10300 9000 12800 17900 15400 26200 11000 8800

TABLE 2 11 12 13 14 15 16 17 18 19 20 Monomer C 2-ethylhexyl methacrylate 136.4 g  lauryl methacrylate 175.0 g  stearyl methacrylate 232.8 g  isobornyl methacrylate 152.9 g  tetrahydrofurfuryl 117.1 g  methacrylate vinyl neononanoate 78.3 g 78.3 g vinyl neodecanoate 84.3 g 84.3 g vinyl neoundecanoate 90.3 g Monomer B 1-vinylimidazole 64.7 g 64.7 g styrene 71.6 g 41.6 g 41.6 g 41.6 g benzyl methacrylate 70.4 g 70.4 g phenethyl methacrylate 130.8 g  2-phenoxyethyl 141.8 g  methacrylate Monomer A polyglcyol 5  210 g polyglycol 6  300 g  300 g  300 g  300 g polyglycol 7 378.4 g  378.4 g  378.4 g  378.4 g  378.4 g  Initiator AMBN 16.5 g 13.4 g 13.4 g 16.5 g 13.4 g 13.4 g dibenzoyl peroxide 20.8 g 20.8 g ascorbic acid/t-BuOOH 17.51 g/ 17.51 g/ 7.73 g 7.73 g Regulator dodecanethiol 13.4 g 16.5 g 13.4 g 16.5 g 13.4 g ethyl mercaptan  4.2 g  4.2 g Solvent methyl ethyl ketone  660 g  660 g  660 g  660 g  660 g  660 g methyl isobutyl ketone  660 g  660 g isopropanol  660 g  660 g to synthesis 1 1 1 1 1 1 1 1 2 2 prescription . . . M_(w) of polymer obtained 16200 7500 6100 8200 14600 7000 15000 8900 14700 9200

TABLE 3 21 22 23 24 25 26 27 28 29 30 Monomer C 2-ethylhexyl methacrylate 136.4 g  lauryl methacrylate 175.0 g  stearyl methacrylate 232.8 g  isobornyl methacrylate 152.9 g  tetrahydrofurfuryl 117.1 g  methacrylate vinyl neononanoate 78.3 g vinyl neodecanoate 84.3 g 84.3 g 78.3 g vinyl neoundecanoate 90.3 g Monomer B 1-vinylimidazole 64.7 g 64.7 g styrene 71.6 g 41.6 g 41.6 g 41.6 g benzyl methacrylate 70.4 g 70.4 g phenethyl methacrylate 130.8 g  2-phenoxyethyl 141.8 g  methacrylate Monomer A polyglcyol 8  300 g  300 g  300 g polyglycol 9  429 g  429 g  429 g polyglycol 10  876 g  876 g polyglycol 11 1224 g  1224 g  Initiator AMBN 16.5 g 13.4 g 13.4 g 16.5 g 13.4 g 13.4 g dibenzoyl peroxide 20.8 g 20.8 g ascorbic acid/t-BuOOH 17.51 g/ 17.51 g/ 7.73 g 7.73 g Regulator dodecanethiol 16.5 g 13.4 g 16.5 g 16.5 g ethyl mercaptan  4.2 g  4.2 g Solvent methyl ethyl ketone  660 g  660 g  660 g  660 g methyl isobutyl ketone  660 g  660 g  660 g  660 g isopropanol  660 g  660 g to synthesis 1 1 1 1 1 1 1 1 2 2 prescription . . . M_(w) of polymer obtained 8400 7900 13900 9000 8100 26200 15000 8600 8900 24800

Monomer A of tables 1 to 3:

-   Polyglycol 1 polyalkylene glycol monovinyl ether (formula (I), k=0,     n=0, m=11.5; (A-O) is (CH₂CH₂O)), molar mass about 550 g/mol -   Polyglycol 2 polyalkylene glycol monovinyl ether (formula (I), k=0,     n=0, m=24; (A-O) is (CH₂CH₂O)), molar mass about 1100 g/mol -   Polyglycol 3 polyalkylene glycol monovinyl ether (formula (I), k=0,     n=0, m=44.5; (A-O) is (CH₂CH₂O)), molar mass about 2000 g/mol -   Polyglycol 4 polyalkylene glycol monovinyl ether (formula (I), k=0,     n=0, m=135.4; (A-O) is (CH₂CH₂O)), molar mass about 6000 g/mol -   Polyglycol 5 polyalkylene glycol monoallyl ether (formula (I), k=1,     n=0, m=6.6; (A-O) is (CH₂CH₂O)), molar mass about 350 g/mol -   Polyglycol 6 polyalkylene glycol monoallyl ether (formula (I), k=1,     n=0, m=10; (A-O) is (CH₂CH₂O)), molar mass about 500 g/mol -   Polyglycol 7 polyalkylene glycol monoallyl ether (formula (I), k=1,     n=0, m=21.4; (A-O) is (CH₂CH₂O)), molar mass about 1000 g/mol -   Polyglycol 8 polyalkylene glycol monoallyl ether (formula (I), k=1,     ethylene oxide/propylene oxide 6:4 (random polymer), molar mass     about 500 g/mol -   Polyglycol 9 polyalkylene glycol monoallyl ether (formula (I), k=1,     ethylene oxide (B—O)/propylene oxide (A-O) 11:4 (block copolymer),     molar mass about 750 g/mol -   Polyglycol 10 polyalkylene glycol monoallyl ether (formula (I), k=1,     ethylene oxide (B—O)/propylene oxide (A-O) 20:10 (block copolymer),     molar mass about 1500 g/mol -   Polyglycol 11 polyalkylene glycol monoallyl ether (formula (I), k=1,     ethylene oxide/propylene oxide 20:20 (random polymer), molar mass     about 2100 g/mol

Production of a Pigment Preparation:

The pigment, in the form alternatively of powder, granulate or presscake, was pasted up in deionized water together with the dispersants and the other adjuvants and then homogenized and predispersed using a dissolver (for example from VMA-Getzmann GmbH, type AE3-M1) or some other suitable apparatus. Fine dispersion was subsequently effected using a bead mill (for example AE3-M1 from VMA-Getzmann) or else some other suitable dispersing assembly, with milling being carried out with siliquartzite beads or zirconium mixed oxide beads of size d=1 mm, accompanied by cooling, until the desired color strength and coloristics were obtained. Thereafter, the dispersion was adjusted with deionized water to the desired final pigment concentration, the grinding media separated off and the pigment preparation isolated.

Evaluation of a Pigment Preparation

Color strength and hue were determined in accordance with DIN 55986. The rub-out test was carried out by applying the emulsion paint or the varnish, after mixing with the pigment dispersion, to a paint card. Subsequently, the applied coating was rubbed with the finger on the lower part of the paint card. Incompatibility was present if the rubbed area is then more strongly or brightly colored than the adjacent area not aftertreated (the rub-out test is described in DE 2 638 946). Color strength and compatibilities with the medium to be colored was determined using 5 different white dispersions:

-   1. white dispersion A (for exteriors, waterborne, 20% TiO₂) -   2. white dispersion B (for exteriors, waterborne, 13.4% TiO₂) -   3. white dispersion C (for exteriors, waterborne, polysiloxane     emulsion as binder, TiO₂, talc, calcium carbonate) -   4. white dispersion D (for interiors, waterborne, polymer     dispersion, free of solvent and plasticizers, low emission, TiO₂,     calcium carbonate) -   5. white dispersion E (for interiors, waterborne, polyacrylates,     TiO₂, calcium carbonate)

Viscosity was determined using a cone-and-plate viscometer (Roto Visco 1) from Haake at 20° C. (titanium cone: Ø 60 mm, 1°), the relationship between viscosity and shear rate in a range between 0 and 200 s⁻¹ being investigated. Viscosities were measured at a shear rate of 60 s⁻¹.

To evaluate the storage stability of the dispersions, viscosity was measured directly after production of the preparation and also after four weeks' storage at 50° C.

Shear stability and foam behavior were observed after shearing a formulation, diluted to 2%, with a commercially available kitchen blender (Braun MX 32) set to a high speed of rotation. The higher the sheer stability of the formulation, the lower the loss of color strength after shearing in a color strength comparison between a sheared versus an unsheared dispersion. Foam behavior was observed after the blender had been turned off.

The pigment preparations described in the examples which follow were produced by the method described above, the following constituents being used in the stated amounts such that 100 parts of the respective pigment preparation are formed. Parts are by weight in the examples below. It is composed of the following general formulation:

-   X parts of component (A), Pigment -   Y parts of component (B), dispersant as per formula (I), (II), (III)     or (IV), the no. of the synthesis example is indicated in the table -   1 part of component (C), lauryl sulfate -   9 parts of component (E), propylene glycol -   0.2 part of component (F), preservative -   Balance component (G), water

The respective fractions of X and Y are reported in the tables which follow.

FS=color strength, comp.=component, P=pigment.

Pigment Test results Test results Test results Test results formulation for white for white for white for white No. Composition dispersion A dispersion B dispersion C dispersion D  1 50 parts P. Blue 15 FS 101% FS 105% FS 100% FS 107% (Comp. A); 8 parts no rub-out, no rub-out, no rub-out, no rub-out, Comp. B from no no no no synthesis example 9 flocculation flocculation flocculation flocculation  2 40 parts P. Black 7 FS 99% FS 100% FS 106% FS 100% (Comp. A); 6 parts slight rub-out, no rub-out, no rub-out, slight rub-out, Comp. B from minimal no no no synthesis example 2 flocculation flocculation flocculation flocculation  3 42 parts P. Red 12 FS 103% FS 103% FS 99% FS 105% (Comp. A); 8 parts no rub-out, no rub-out, no rub-out, no rub-out, Comp. B from no minimal no no synthesis example 19 flocculation flocculation flocculation flocculation  4 45 parts P. Green 7 FS 102% FS 100% FS 99% FS 103% (Comp. A); 8 parts no rub-out, slight rub-out, no rub-out, no rub-out, Comp. B from no no slight no synthesis example 16 flocculation flocculation flocculation flocculation  5 50 parts P. Red 112 FS 99% FS 95% FS 105% FS 101% (Comp. A); 8 parts no rub-out, no rub-out, no rub-out, no rub-out, Comp. B from no no no no synthesis example 26 flocculation flocculation flocculation flocculation  6 40 parts P. Red 168 FS 102% FS 103% FS 102% FS 104% (Comp. A); 9 parts no rub-out, slight rub-out, no rub-out, minimal Comp. B from no no no rub-out, no synthesis example 5 flocculation flocculation flocculation flocculation  7 50 parts P. Yellow 1 FS 100% FS 100% FS 102% FS 101% (Comp. A); 10 parts no rub-out, no rub-out, no rub-out, no rub-out, Comp. B from no minimal no no synthesis example 13 flocculation flocculation flocculation flocculation  8 40 parts P. Yellow 83 FS 95% FS 98% FS 98% FS 102% (Comp. A); 7 parts no rub-out, no rub-out, no rub-out, no rub-out, Comp. B from no no no no synthesis example 22 flocculation flocculation flocculation flocculation  9 45 parts P. Blue 15:1 FS 104% FS 100% FS 103% FS 102% (Comp. A); 6 parts no rub-out, no rub-out, no rub-out, no rub-out, Comp. B from no no no no synthesis example 30 flocculation flocculation flocculation flocculation.0 10 40 parts P. Red 5 FS 99% FS 94% FS 103% FS 107% (Comp. A); 8 parts no rub-out, no rub-out, no rub-out, minimal rub- Comp. B from no no no out, no synthesis example 15 flocculation flocculation flocculation flocculation 11 65 parts P. White 6 103% relative — — — (Comp. A); 8 parts whitening Comp. B from power in black synthesis example 1 emulsion paint 12 47 parts P. Blue 15:3 FS 100% FS 100% FS 100% FS 102% (Comp. A); 7.5 parts no rub-out, no rub-out, no rub-out, no rub-out, Comp. B from no no no no synthesis example 12 flocculation flocculation flocculation flocculation 13 40 parts P. Orange 36 FS 105% FS 100% FS 105% FS 101% (Comp. A); 8 parts no rub-out, no rub-out, no rub-out, no rub-out, Comp. B from no no no no synthesis example 21 flocculation flocculation flocculation flocculation 14 38 parts P. Red 122 FS 108% FS 105% FS 102% FS 105% (Comp. A); 11 parts no rub-out, no rub-out, no rub-out, no rub-out, Comp. B from no no no no synthesis example 16 flocculation flocculation flocculation flocculation 15 50 parts P. Red 3 FS 98% FS 99% FS 89% FS 100% (Comp. A); 10 parts no rub-out, no rub-out, no rub-out, no rub-out, Comp. B from no no no no synthesis example 28 flocculation flocculation flocculation flocculation 16 35 parts P. Violet 19 FS 104% FS 102% FS 102% FS 100% (Comp. A); 7 parts no rub-out, no rub-out, no rub-out, no rub-out, Comp. B from no no no no synthesis example 24 flocculation flocculation flocculation flocculation 17 50 parts P. Red 254 FS 101% FS 100% FS 102% FS 104% (Comp. A); 8 parts no rub-out, no rub-out, no rub-out, no rub-out, Comp. B from no no no minimal synthesis example 3 flocculation flocculation flocculation flocculation 18 45 parts P. Orange 5 FS 100% FS 102% FS 105% FS 101% (Comp. A); 12 parts no rub-out, no rub-out, minimal rub- no rub-out, Comp. B from no no out, no minimal synthesis example 29 flocculation flocculation flocculation flocculation 19 48 parts P. Red 9 FS 98% FS 102% FS 100% FS 105% (Comp. A); 7 parts no rub-out, no rub-out, no rub-out, no rub-out, Comp. B from no no no minimal synthesis example 17 flocculation flocculation flocculation flocculation 20 40 parts P. Red 188 FS 103% FS 100% FS 102% FS 108% (Comp. A); 10.5 parts no rub-out, no rub-out, no rub-out, minimal rub- Comp. B from no no no out, no synthesis example 14 flocculation flocculation flocculation flocculation 21 36 parts P. Violet 23 FS 95% FS 96% FS 99% FS 94% (Comp. A); 12 parts no rub-out, no rub-out, minimal rub- no rub-out, Comp. B from no no out, no no synthesis example 23 flocculation flocculation flocculation flocculation 22 50 parts P. Yellow 74 FS 102% FS 107% FS 101% FS 102% (Comp. A); 9 parts no rub-out, slight rub- no rub-out, no rub-out, Comp. B from no out, no no no synthesis example 27 flocculation flocculation flocculation flocculation 23 48 parts P. Yellow 97 FS 100% FS 101% FS 103% FS 101% (Comp. A); 10 parts no rub-out, no rub-out, no rub-out, no rub-out, Comp. B from no no no no synthesis example 20 flocculation flocculation flocculation flocculation 24 40 parts P. Yellow 154 FS 106% FS 100% FS 101% FS 98% (Comp. A); 10 parts no rub-out, slight rub- no rub-out, no rub-out, Comp. B from no out, no no no synthesis example 25 flocculation flocculation flocculation flocculation 25 45 parts P. Yellow 16 FS 99% FS 102% FS 106% FS 100% (Comp. A); 12 parts no rub-out, no rub- no rub-out, no rub-out, Comp. B from no out, minimal no no synthesis example 10 flocculation flocculation flocculation flocculation 26 42 parts P. Red 170 FS 101% FS 102% FS 102% FS 102% (Comp. A); 10 parts no rub-out, no rub- no rub-out, no rub-out, Comp. B from no out, no no no synthesis example 6 flocculation flocculation flocculation flocculation 27 45 parts P. Red 184 FS 100% FS 100% FS 100% FS 100% (Comp. A); 8 parts no rub-out, no rub- no rub-out, minimal rub- Comp. B from no out, no minimal out, no synthesis example 4 flocculation flocculation flocculation flocculation 28 40 parts P. Red 188 FS 106% FS 100% FS 95% FS 99% (Comp. A); 12 parts no rub-out, no rub-out, slight rub- no rub-out, Comp. B from no no out, no no synthesis example 11 flocculation flocculation flocculation flocculation 29 41 parts P. Violet 32 FS 103% FS 104% FS 105% FS 102% (Comp. A); 7 parts no rub-out, no rub-out, no rub-out, no rub-out, Comp. B from no no no no synthesis example 18 flocculation flocculation flocculation flocculation 30 40 parts P. Brown 25 FS 99% FS 98% FS 99% FS 105% (Comp. A); 8 parts no rub-out, no rub-out, no rub-out, no rub-out, Comp. B from no no no no synthesis example 7 flocculation flocculation flocculation flocculation 31 42 parts P. Brown 41 FS 100% FS 100% FS 103% FS 104% (Comp. A); 9 parts no rub-out, no rub-out, no rub-out, minimal rub- Comp. B from no slight no out, no synthesis example 8 flocculation flocculation flocculation flocculation 32 45 parts P. Red 208 FS 108% FS 106% FS 102% FS 106% (Comp. A); 10 parts some rub-out, no rub-out, no rub-out, no rub-out, Comp. B from minimal no no no synthesis example 24 flocculation flocculation flocculation flocculation 33 38 parts P. Yellow 151 FS 100% FS 102% FS 101% FS 105% (Comp. A); 10 parts no rub-out, no rub-out, no rub-out, minimal rub- Comp. B from no minimal no out, no synthesis example 1 flocculation flocculation flocculation flocculation 34 40 parts P. Black 11 FS 102% FS 102% FS 103% FS 104% (Comp. A); 5 parts no rub-out, no rub-out, no rub-out, no rub-out, Comp. B from no no no no synthesis example 16 flocculation flocculation flocculation flocculation 35 65 parts P. Blue 28 FS 99% FS 97% FS 98% FS 99% (Comp. A); 5 parts no rub-out, rub-out, no rub-out, no rub-out, Comp. B from no no no no synthesis example 17 flocculation flocculation flocculation flocculation 36 50 parts P. Green 50 FS 100% FS 101% FS 100% FS 104% (Comp. A); 6 parts no rub-out, no rub-out, no rub-out, no rub-out, Comp. B from no no no no synthesis example 20 flocculation flocculation flocculation flocculation 37 75 parts P. Green 17 FS 100% FS 102% FS 102% FS 96% (Comp. A); 5 parts no rub-out, no rub-out, no rub-out, no rub-out, Comp. B from no no no no synthesis example 12 flocculation flocculation flocculation flocculation 38 70 parts P. Red 101 FS 100% FS 102% FS 103% FS 102% (Comp. A); 5 parts no rub-out, no rub-out, no rub-out, minimal Comp. B from no no no rub-out, no synthesis example 29 flocculation flocculation flocculation flocculation 39 65 parts P. Yellow 184 FS 98% FS 102% FS 105% FS 99% (Comp. A); 8 parts no rub-out, no rub-out, no rub-out, minimal Comp. B from no no no rub-out, no synthesis example 13 flocculation flocculation flocculation flocculation Pigment Test results formulation for white Shear Foam As-prepared No. dispersion E stability behavior viscosity Storage stability  1 FS 100% very good no significant 573 mPas very good no rub-out, foam observed no flocculation  2 FS 98% very good no significant 346 mPas good no rub-out, foam observed no flocculation  3 FS 101% good no significant 610 mPas very good no rub-out, foam observed no flocculation  4 FS 100% very good no significant 492 mPas very good no rub-out, foam observed no flocculation  5 FS 105% very good slight foaming 344 mPas very good no rub-out, observed no flocculation  6 FS 103% very good no significant 407 mPas good no rub-out, foam observed no flocculation  7 FS 97% very good no significant 264 mPas very good no rub-out, foam observed no flocculation  8 FS 98% good slight 224 mPas very good no rub-out, foaming no observed flocculation  9 FS 102% very good no significant 205 mPas very good no rub-out, foam observed minimal flocculation 10 FS 99% good a few foam 658 mPas good enough no rub-out, bubbles no observed flocculation 11 — very good no significant 1494 mPas  very good foam observed 12 FS 100% very good no significant 210 mPas very good no rub-out, foam observed no flocculation 13 FS 101% very good no significant 680 mPas very good no rub-out, foam observed no flocculation 14 FS 108% good no significant 641 mPas very good no rub-out, foam observed no flocculation 15 FS 96% good slight foaming 224 mPas very good no rub-out, enough observed no flocculation 16 FS 99% very good no significant 910 mPas very good no rub-out, foam observed no flocculation 17 FS 102% very good no significant 509 mPas very good no rub-out, foam observed no flocculation 18 FS 96% very good no significant 750 mPas very good no rub-out, foam observed no flocculation 19 FS 99% very good no significant 381 mPas very good no rub-out, foam observed no flocculation 20 FS 103% very good no significant 600 mPas very good no rub-out, foam observed no flocculation 21 FS 95% very good no significant 163 mPas very good no rub-out, foam observed no flocculation 22 FS 101% good slight foaming 308 mPas very good no rub-out, observed no flocculation 23 FS 96% very good no significant 461 mPas very good no rub-out, foam observed no flocculation 24 FS 99% very good no significant 540 mPas good no rub-out, foam observed no flocculation 25 FS 97% very good no significant 434 mPas very good no rub-out, foam observed no flocculation 26 FS 99% very good no significant 807 mPas good no rub-out, foam observed no flocculation 27 FS 105% very good no significant 367 mPas very good no rub-out, foam observed no flocculation 28 FS 104% good no significant 679 mPas very good no rub-out, foam observed no flocculation 29 FS 99% good no significant 600 mPas good no rub-out, foam observed no flocculation 30 FS 103% very good no significant 604 mPas very good no rub-out, foam observed no flocculation 31 FS 102% very good no significant 499 mPas very good no rub-out, foam observed no flocculation 32 FS 95% very good no significant 816 mPas very good no rub-out, foam observed no flocculation 33 FS 102% very good no significant 260 mPas very good no rub-out, foam observed no flocculation 34 FS 105% very good no significant 1588 mPas  very good no rub-out, foam observed no flocculation 35 FS 102% good no significant 1890 mPas  very good no rub-out, foam observed no flocculation 36 FS 100% very good slight foam 2347 mPas  very good no rub-out, observed no flocculation 37 FS 99% very good no significant 2108 mPas  very good no rub-out, foam observed no flocculation 38 FS 101% very good no significant 1764 mPas  very good no rub-out, foam observed no flocculation 39 FS 106% good no significant 2590 mPas  very good no rub-out, foam observed no flocculation 

1. An aqueous pigment preparation comprising (A) at least one organic pigment, an inorganic pigment or a mixture thereof, (B) a dispersant of formula (I), (II), (III) or (IV) or mixtures of dispersants of formulae (I), (II), (III) or (IV)

wherein the indices a, b and c are the molar fraction of the respective monomers: a=0.01 to 0.8; b=0.001 to 0.8; c=0.001 to 0.8; provided the sum total of a+b+c is 1, A is C₂- to C₄-alkylene and B is a C₂- to C₄-alkylene other than A, k equals 0 or 1, m is from 0 to 500; n is from 0 to 500, provided the sum total of m+n is from 1 to 1000; X_(a) is an aromatic or araliphatic radical having 3 to 30 carbon atoms optionally containing one or more of the hetero atoms N, O and S, Z_(a) is H or (C₁-C₄)-alkyl, Z_(b) is H or (C₁-C₄)-alkyl, Z_(c) is H or (C₁-C₄)-alkyl; R¹ is hydrogen or methyl, X_(b) is an aromatic or araliphatic radical having 3 to 30 carbon atoms optionally containing one or more of the hetero atoms N, O and S, W_(a) is oxygen or an NH group, R² is hydrogen or methyl, Y is an aliphatic hydrocarbyl radical having 1 to 30 carbon atoms, which is optionally linear or branched or else cyclic, and optionally contains hetero atoms O, N, S or a mixture thereof and optionally unsaturated, W_(b) is oxygen or an NH group; (C) optionally wetters, (D) optionally at least one surfactant, at least one dispersant or a mixture thereof, (E) optionally one or more organic solvents, one or more hydrotropic substances or a mixture thereof, (F) optionally further additive materials customary for preparing aqueous pigment dispersions, and (G) water.
 2. The pigment preparation as claimed in claim 1, comprising 5% to 80% by weight of said component (A).
 3. The pigment preparation as claimed in claim 1, comprising 0.1% to 30% by weight of said component (B).
 4. The pigment preparation as claimed in claim 1, having the following composition of said components (A) to (G): (A) 5% to 80% by weight, (B) 0.1% to 30% by weight, (C) 0% to 10% by weight, (D) 0% to 20% by weight, (E) 0% to 30% by weight, (F) 0% to 20% by weight, (G) 1% to 90% by weight of water, all based on the total weight of said pigment preparation.
 5. The pigment preparation as claimed in claim 1, having the following composition of said components (A) to (G): (A) 10% to 70% by weight, (B) 2% to 15% by weight, (C) 0.1% to 5% by weight, (D) 1% to 10% by weight, (E) 5% to 20% by weight, (F) 0.1% to 5% by weight, (G) 10% to 70% by weight of water, all based on the total weight of said pigment preparation.
 6. The pigment preparation as claimed in claim 1, wherein the organic pigment of said component (A) is a monoazo, disazo, laked azo, β-naphthol, Naphthol AS, benzimidazolone, disazo condensation, azo metal complex pigment or a polycyclic pigment selected from the group consisting of phthalocyanine, quinacridone, perylene, perinone, thioindigo, anthanthrone, anthraquinone, flavanthrone, indanthrone, isoviolanthrone, pyranthrone, dioxazine, quinophthalone, isoindolinone, isoindoline and diketopyrrolopyrrole pigments or carbon blacks.
 7. The pigment preparation as claimed in claim 1, wherein the alkylene oxide units (A-O)_(m) and (B—O)_(n) are arranged blocklike in said component (B).
 8. A process for producing a pigment preparation as claimed in claim 1, comprising the steps of dispersing said component (A) in the form of powder, granulate or aqueous presscake in the presence of water (G) and also said components (B) and optionally (C) and (D), optionally admixing water (G), optionally one or more of said components (E) and (F) and optionally diluting the resulting aqueous pigment dispersion with water (G); or precharging said components (B) and optionally mixing and homogenizing one or more of said components (C), (D), (E) and (F) to form an initially charged mixture, stirring said component (A) into the initially charged mixture, said component (A) being incipiently pasted and predispersed.
 9. A natural or synthetic material pigmented by a pigment preparation as claimed in claim
 1. 10. A pigmented aqueous paint, dispersion color varnish color, water-thinnable varnish, wallpaper color or printing color pigmented by the pigment preparation as claimed in claim
 1. 11. A pigmented composition pigmented by a pigment preparation as claimed in claim 1, wherein the pigmented composition is in a form selected from the group consisting of natural fiber materials, synthetic fiber materials, cellulose fibers, paper pulp, laminate, printing inks, ink-jet inks, electrophotographic toners, powder coatings, color filters, electronic inks electronic paper, color filters, wood preservation systems, viscose dope dyeing, sausage casings, seed, fertilizers, glass bottles, roof shingles, renders, concrete, wood stains, colored pencil leads, felt tip pens, waxes, paraffins, graphics inks, ballpoint pen pastes, chalks, washing compositions, cleaning compositions, shoe care agents, latex products, abrasives, plastics.
 12. The pigment preparation as claimed in claim 1, the aliphatic hydrocarbyl radical has 6 to 30 carbon atoms.
 13. The pigment preparation as claimed in claim 1, wherein the aliphatic hydrocarbyl radical has 9 to 20 carbon atoms. 